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Review: could Nicotine cause Neuropathy peripheral?

Summary: Neuropathy peripheral is found among people who take Nicotine, especially for people who are male, 50-59 old, also take medication Neurontin, and have Stress and anxiety.

We study 5,665 people who have side effects while taking Nicotine from FDA and social media. Among them, 22 have Neuropathy peripheral. Find out below who they are, when they have Neuropathy peripheral and more.

You are not alone: join a mobile support group for people who take Nicotine and have Neuropathy peripheral >>>

 

 

 

 

Nicotine

Nicotine has active ingredients of nicotine. It is often used in quit smoking. (latest outcomes from 5,796 Nicotine users)

Neuropathy peripheral

Neuropathy peripheral (surface nerve damage) has been reported by people with multiple myeloma, osteoporosis, depression, pain, high blood pressure. (latest reports from 27,673 Neuropathy peripheral patients)

On Jan, 24, 2015: 5,665 people reported to have side effects when taking Nicotine. Among them, 22 people (0.39%) have Neuropathy Peripheral.

Trend of Neuropathy peripheral in Nicotine reports

Time on Nicotine when people have Neuropathy peripheral * :

n/a

Gender of people who have Neuropathy peripheral when taking Nicotine * :

FemaleMale
Neuropathy peripheral47.62%52.38%

Age of people who have Neuropathy peripheral when taking Nicotine * :

0-12-910-1920-2930-3940-4950-5960+
Neuropathy peripheral0.00%0.00%0.00%0.00%5.26%15.79%68.42%10.53%

Severity of Neuropathy peripheral when taking Nicotine ** :

n/a

How people recovered from Neuropathy peripheral ** :

n/a

Top conditions involved for these people * :

  1. Anxiety (8 people, 36.36%)
  2. Multiple myeloma (8 people, 36.36%)
  3. Smoking cessation therapy (7 people, 31.82%)
  4. Depression (5 people, 22.73%)
  5. Agitation (4 people, 18.18%)

Top co-used drugs for these people * :

  1. Neurontin (14 people, 63.64%)
  2. Zometa (11 people, 50.00%)
  3. Protonix (11 people, 50.00%)
  4. Nexium (10 people, 45.45%)
  5. Chemotherapeutics nos (10 people, 45.45%)

* Approximation only. Some reports may have incomplete information.

** Reports from social media are used.

How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.

Do you have Neuropathy Peripheral while taking Nicotine?

You are not alone! Join a mobile support group:
- support group for people who take Nicotine and have Neuropathy Peripheral
- support group for people who take Nicotine
- support group for people who have Neuropathy Peripheral

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You may be interested at these reviews (Write a review):

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    So...

    In 1997 I was diagnosed with Narcolepsy with an intolerance to Dexamp(hetamine) tablets.

    After 3 years of nose operations, and sleep tests to remove other potential issues (lung problems or apnoea) I have finally been re-diagnosed (2013) with idiopathic insomnolence.

    Modaphinil caused a reaction of insane nausea, pains behind the eyes, dizzy spells, with no real change in blood pressure.

    Dexamphetamine was erratic (on recent retrial) with extremes causing dizzy spells and slow progressive drop in BP over 3 weeks from average 125/75 to 105/60. Occasionally it would wake my body up but my brain would be slow to follow, and the conflict would take me to the cleaners for the next two days.

    I was diagnosed with IgAN in 2004, and have progressive idiopathic neuropathy in my feet since 2011.

    The sleep specialist wants me to try Klacid (clarithromycin) as it has reportedly caused insomnia on a regular basis. I've not yet agreed.

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    To many idiopathics and drug rejections.

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    I was prescribed that combination of drugs in January 2013 when I went to my family doctor with a bad chest congestion and painful knees. After starting on the drugs, I got a severely painful neck and thumb and noticed some tingling in my left foot. I took the whole course of the avelox and prednisone, though I discontinued the nabumetome. I kept getting weaker and weaker till I could hardly walk. I ended up in the emergency room and was first diagnosed with Rhabdomyolysis but rushed to a bigger hospital for further diagnosis and treatment. I was close to needing blood, my kidneys were shutting down and I could barely walk. I was so weak! My right hand and left foot went "to sleep" and still haven't woken up. ( as of October 2013)

    After many, many tests, they came up with a tentative diagnosis of vasculitis and myositis.

    Then I had a kidney biopsy which confirmed the vasculitis and I was immediately treated with chemotherapy -- cytoxin for 6 months.

    IAlthough I do feel much better, I am still suffering and taking drugs for the vasculitis and I am told that I may go into remission, but it could flare up again anytime. I am convinced that it was the drug combination that caused all this. I had been feeling great and had a daily walking routine of walking 2 to 5 miles per day, and no other complaints.

    The nephrologist did say that while it might be that the vasculitis was drug induced, it didn't matter because I have it and he's treating it and would be doing it this way no matter how I got it.

    When I told my family doctor that I thought it was the drug combination that caused my problems, he seemed surprised and really no discussion. I told them to put it in my medical records to NEVER give me a flouroquinolone drug again.

    Yesterday when I went for a blood test and urinalysis ( which I was doing biweekly, but now every 6 weeks), it showed that I have a UTI and guess what the family doctor called in a prescription for? Cipro!!!! And he knows I'm still on prednisone and have only 30% kidney function!!!!!!

    While I am not a litigious person, this really makes me so upset!!! I don't have the money to try to sue, but if telling my story will help keep unsuspecting people from the horrible damage this has caused, I feel obligrdmtomspeak up. I have had a terrible year. And I'm still not okay. And the drugs 'm taking make me susceptible to other problems. I'm still all puffed up from the prednisone. A couple of weeks ago I decided to try going for walks again, hopefully to lose some of this weight and build up my strength. It is so hard for me and my left foot hurts so bad. My legs feel so heavy it is a real struggle to walk a mile. But at least I can. When I was at my sickest, could barely walk to the bathroom and I could not get up from the toilet without using my arms to pull myself up. I couldn't go up the two steps to get into my house without help. I couldn't go upstairs to my bedroom for months.

More reviews for: Nicotine, Neuropathy peripheral

Comments from related studies:

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  • Incontinence is intermittent. I thought it was related to a UTI. But it has persisted for almost a year, on and off. It has been two months since intercourse. I assume I must rule out a UTI. I smoke an e cigarette which appears to have no effect, as I've used it the entire time since the incontinence first started and the incontinence symptoms have come and gone.

    I am currently tapering off the paxil, hoping the incontinence will stop. The incontinence seems to get worse when I experience withdrawal symptoms suck as dizziness. Or this bizarre symptom that I can only explain as micro seizures. When the incontinence gets worse, I do not consume alcohol or soda. I try to drink a lot of water, juices and tea.

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  • From this study (7 months ago):

  • My friend recently wanted me to quit smoking, so he got me a ecigarette so it is less harmful. I now use it more than i usually smoke because i can use it in the house. Before i had to go outside to have a smoke, now i can read a book or watch tv with it right in front of me and avoid the hassle of going outside. Because of the convenience, i use it fairly regularly in side.

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